Literature DB >> 30779856

Meta-Analysis of Genome-Wide Association Studies Identifies Three Loci Associated With Stiffness Index of the Calcaneus.

Hsing-Fang Lu1,2, Kuo-Sheng Hung3,4,5, Hou-Wei Chu6, Henry Sung-Ching Wong1,3, Jihye Kim7,8, Mi Kyung Kim7,8, Bo Youl Choi7,8, Yu-Ting Tai9, Shiro Ikegawa2, Er-Chieh Cho1,3,10, Wei-Chiao Chang1,3,11,12,13.   

Abstract

The stiffness index (SI) from quantitative ultrasound measurements is a good indicator of BMD and may be used to predict the risk of osteoporotic fracture. We conducted a genomewide association study (GWAS) for SI using 7742 individuals from the Taiwan Biobank, followed by a replication study in a Korean population (n = 2955). Approximately 6.1 million SNPs were subjected to association analysis, and SI-associated variants were identified. We further conducted a meta-analysis of Taiwan Biobank significant SNPs with a Korean population-based cohort. Candidate genes were prioritized according to epigenetic annotations, gene ontology, protein-protein interaction, GWAS catalog, and expression quantitative trait loci analyses. Our results revealed seven significant single-nucleotide polymorphisms (SNPs) within three loci: 7q31.31, 17p13.3, and 11q14.2. Conditional analysis showed that three SNPs, rs2536195 (CPED1/WNT16), rs1231207 (SMG6), and rs4944661 (LOC10050636/TMEM135), were the most important signals within these regions. The associations for the three SNPs were confirmed in a UK Biobank estimated BMD GWAS; these three cytobands were replicated successfully after a meta-analysis with a Korean population cohort as well. However, two SNPs were not replicated. After prioritization, we identified two novel genes, RAB15 and FNTB, as strong candidates for association with SI. Our study identified three SI-associated SNPs and two novel SI-related genes. Overall, these results provide further insight into the genetic architecture of osteoporosis. Further studies in larger East Asian populations are needed.
© 2019 American Society for Bone and Mineral Research. © 2019 American Society for Bone and Mineral Research.

Entities:  

Keywords:  GENOME-WIDE ASSOCIATION STUDY; HEEL BONE MINERAL DENSITY; OSTEOPOROSIS; STIFFNESS INDEX; TAIWAN BIOBANK

Year:  2019        PMID: 30779856     DOI: 10.1002/jbmr.3703

Source DB:  PubMed          Journal:  J Bone Miner Res        ISSN: 0884-0431            Impact factor:   6.741


  3 in total

1.  Deficiency of TMEM53 causes a previously unknown sclerosing bone disorder by dysregulation of BMP-SMAD signaling.

Authors:  Long Guo; Aritoshi Iida; Gandham SriLakshmi Bhavani; Kalpana Gowrishankar; Zheng Wang; Jing-Yi Xue; Juan Wang; Noriko Miyake; Naomichi Matsumoto; Takanori Hasegawa; Yusuke Iizuka; Masashi Matsuda; Tomoki Nakashima; Masaki Takechi; Sachiko Iseki; Shinsei Yambe; Gen Nishimura; Haruhiko Koseki; Chisa Shukunami; Katta M Girisha; Shiro Ikegawa
Journal:  Nat Commun       Date:  2021-04-06       Impact factor: 14.919

2.  Pharmacogenomics Study for Raloxifene in Postmenopausal Female with Osteoporosis.

Authors:  Hsing-Fang Lu; Po-Hsin Chou; Gan-Hong Lin; Wan-Hsuan Chou; Shih-Tien Wang; Wirawan Adikusuma; Eko Mugiyanto; Kuo-Sheng Hung; Wei-Chiao Chang
Journal:  Dis Markers       Date:  2020-08-31       Impact factor: 3.434

Review 3.  The Polygenic and Monogenic Basis of Paediatric Fractures.

Authors:  S Ghatan; A Costantini; R Li; C De Bruin; N M Appelman-Dijkstra; E M Winter; L Oei; Carolina Medina-Gomez
Journal:  Curr Osteoporos Rep       Date:  2021-05-04       Impact factor: 5.096

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.